People living with ET and taking Hydrea: Anybody setting records?
I've been wondering if there are any stats on people who have lived the longest with ET and taking Hydrea? As I hit the 30-year mark soon, I'd like to know about long-term survivors! 🙂 Guess I'm looking for some encouragement--haha!
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International Prognostic Score for ET
Patient age less than 60 (0 points)
Older than 60 (1 point)
Prior thrombotic event
No: (0 points). Yes: (2 points)
Cardio vascular risks factors
No: (0 points). Yes: ( 1 point)
JAK2 V617 mutation detected
No: (0 points). Yes: (2 points)
Low risk is 0-1
Intermediate is 2
high is 3-6
Eileen
I was diagnosed with ET and I now take Hydrea and .81 aspirin looking for as much information
Any specific questions?
Well, I think I fall into the high risk category, as I'm older than 60, have had a thrombotic event and have the JAK2 mutation. But I've been on HU 500 mg since I was 39. So I'm closing in on 30 years with the dx and taking HU. I feel fine. Just saw my hematologist and I don't see any reasons I won't go on for quite some time yet!
I’m just so worried about “what are my platelet levels” is the medicine safe. I don’t want to have a stroke. I’m often fatigued, headache and nauseous. It’s scary
"At 82 yes I would like to keep other parts of me as healthy as possible.
(also, recently had hip replacement surgery so have been recovering from that, with Physio etc) I think that is probably the case with most of us, that the Essential Thrombocythemia is not the only thing going on. "
Very true. I have severe scoliosis (congenital spinal curvature) that causes nerve tingles, and a bad heart valve that causes dizziness. These are also symptoms of ET. I presume the migraines w flashing lights and fatigue are ET symptoms. These are better since I started HU.
Encouraged to hear you had major surgery with ET while taking HU. A mitral valve repair is in my near future. They are talking open-heart surgery, but I am hoping to make it to 70 (I'm 68) so I can have the trans cath procedure. Quicker recovery time, which would be much easier on my back. Given that the back problem will worsen with time, I'm less about living a long time than maximizing the quality of my time.
When were you diagnosed? How old were you? I remember worrying about the safety of the HU, but when I quit HU and experienced a TIA, I came to peace with it and decided the HU was safer for me than going without. After that, I made a conscious choice to quit the worrying and constant research and just live life. In fact, I don't even think about it anymore after 30 years. Depending on how long you've been on the HU, I would wonder how much anxiety creates your symptoms, as anxiety definitely takes a physical toll. It's hard to say if it's the disease or the meds causing the symptoms. But I'd like to know more about your journey!
Diagnosed 11/19/2022 and started the med. The hematologist was watching the platelet level for the past 5 years. Red platelets reached 915 in November. I’m 68 years old I go to the gym daily and work per diem as a social worker.
What is TIAs?
Stands for transient ischemic attack. Sometimes called mini strokes. They mimic stroke symptoms but resolve quickly and may be precursors to strokes: https://www.mayoclinic.org/diseases-conditions/transient-ischemic-attack/symptoms-causes/syc-20355679